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NCT01375543 · ClinicalTrials.gov registry record

Next Generation to Identify Genetic Causes of Disease in Patients Participating in NICHD Clinical Protocols

A clinical trial, sponsored by Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD).

Completed
Registry status
128
Enrollment target

NCT01375543: Completed study, sponsored by Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD).

NCT01375543 is a clinical trial that has completed, run by Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD). The registered enrollment target is 128 participants. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT01375543 has completed, sponsored by Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD).

COMPLETED
Registry status
128 participants
Enrollment target

Study Summary

Background: \- The purpose of this study is to identify changes in genes that cause human diseases. We would like to obtain some of you or your child s DNA and test for changes in genes that may contribute to a disease in you or your family. Objective: -To allow for exomic or genomic sequencing of NICHD patients or family members in order to identify changes in genes that cause or contribute to a specific disease. Eligibility: * Children who are enrolled in an NICHD clinical study where the condition being studied may have a genetic cause. * Family members of a child who is eligible for this study. Design: * Children and family members will supply DNA samples. If the samples are already available, no further DNA will be needed. * If DNA is not available, samples of either blood or skin will be taken. * We will use these samples with new DNA sequencing technology that looks at all the human genes we know about. This is known as exome and genome sequencing.

Primary Outcome

Identify genetic causes of rare diseases

Trial Details

FieldValue
Enrollment Target 128 participants
Start Date 2011-06-16
Est. Completion 2019-12-31

What the finished NCT01375543 record still lists

NCT01375543 is an observational study that tracks outcomes without assigning an intervention. The registered 128 participants enrollment target is mid-sized for trials with a published cap.

The record links to 0 conditions, and to 0 interventions.

NCT01375543 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT01375543 about?

NCT01375543 is a clinical study titled "Next Generation to Identify Genetic Causes of Disease in Patients Participating in NICHD Clinical Protocols". Background: \- The purpose of this study is to identify changes in genes that cause human diseases. We would like to obtain some of you or your child s DNA and test for changes in genes that may contribute to a disease in you or your family. Objective: -To allow for exomic or genomic sequencing o...

What is the current status of trial NCT01375543?

This trial is currently completed. The enrollment target is 128 participants. The study started on 2011-06-16. Estimated completion is 2019-12-31.

Who is sponsoring clinical trial NCT01375543?

This trial is sponsored by Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD), which has 305 total clinical trials registered on ClinicalTrials.gov.

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Source: ClinicalTrials.gov NCT01375543, the US trial registry maintained by the National Library of Medicine. NCT01375543 (mid enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.